Flexible to rigid nanoporous polyurethane-acrylate (PUAC) type materials for structural and thermal insulation applications

ABSTRACT

Novel urethane-acrylate (UAC) Star monomers and polyurethane-acrylate (PUAC) aerogel polymers derived therefrom are described herein, along with other novel, related monomers and polymers. Also described herein are processes for preparing the UAC Star monomers, the PUAC aerogel polymers, and the other related monomers and polymers. The PUAC and related polymers herein are useful in various applications including in structural and thermal insulation.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of, and claims priority to,co-pending U.S. patent application Ser. No. 14/208,892, filed on Mar.13, 2014, the entire disclosure of which is incorporated herein byreference.

GOVERNMENT RIGHTS

This invention was made with Government support under Grant No.CHE-0809562 awarded by the National Science Foundation and Grant No.W911NF-10-1-0476 awarded by the Army Research Office. The U.S.government has certain rights in the invention.

TECHNICAL FIELD

The present invention relates, inter alia, to structural insulationmaterials, thermal insulation materials, and similar materials. Morespecifically, the present invention relates to a series of nanoporouspolyurethane-acrylate type materials and similar materials forapplications in structural insulation, thermal insulation, and the like.

BACKGROUND AND SUMMARY OF THE INVENTION

In one embodiment, the present invention discloses a series ofnanoporous polyurethane-acrylate (PUAC) type materials for applicationsin structural insulation, thermal insulation, and the like. In anotherembodiment, the present invention discloses a series ofurethane-acrylate (UAC) Star monomers, which are monomeric precursorsfor the preparation of the PUAC materials. In yet another embodiment,the present invention discloses one or more processes for the conversionof the UACs to their corresponding PUACs. In yet another embodiment, thepresent invention discloses methods of use of the PUACs as aerogelmaterials for applications in structural insulation, thermal insulation,and the like.

Aerogels have been known as three-dimensional lightweight porousmaterials formed by aggregation of nanoparticles, wherein the thicknessdimension may vary greatly (from nanometers to meters) such that in somecases they may be viewed as quasi-two-dimensional objects. High surfaceareas and open porosities have been reported as being two of the mostattractive properties for applications in thermal insulation, drugdelivery, catalysis, and other applications. Aerogels are believed tohave been first reported in 1931 by Kistler, who is believed to haveintroduced supercritical fluid (SCF) drying as a means to retain thenetwork morphology of wet-gels into the final dry objects. Mostpost-Kistler attention appears to have focused on silica aerogels.Organic aerogels seem to have started getting attention after thesynthesis of resorcinol-formaldehyde (RF) aerogels.

For a number of years, polymer- and RF-aerogels were almost synonymousterms. In the last few years, however, research on other polymer-basedaerogels seems to have gained significant momentum. It is believed thatthe reasons include well-defined chemistry, molecular designflexibility, readily available raw materials, and the excellentmechanical, thermal, chemical, and other properties of these polymers.

In another embodiment, described herein are polymer aerogels obtained byusing polyurethane-acrylate (PUAC) chemistry. PUAC polymers have beenpopular in the automotive and coating industries. It is believed thatthis is so because PUAC polymers incorporate properties of bothpolyurethanes and polyacrylates, and because they can be prepared easilyby free-radical polymerization using UV light or heat. It has beenobserved that low density PUAC aerogels tend to be flexible, whilehigher density PUAC aerogels tend to possess greater stiffness andstronger mechanical properties.

It has been reported that flexible aerogels are interesting for aplethora of applications, illustratively, in planetary descent andlanding (EDL) systems, thermal insulation, such as in sub-sea oil pipes(e.g., see http://www.aerogel.com/markets/subsea.html) and buildings(e.g., acoustic insulation), where flexibility and foldability areconsidered to be necessary properties. It has also been reported thatthe impressive strength-to-weight ratio of higher-density PUAC aerogelsrenders them attractive as energy absorbers for defense applications.

In another embodiment of the invention herein, thermally stable PUACaerogels are described. In one aspect, the thermal stability of thesePUAC aerogels can be as high as 300° C. In another aspect, the thermallystable PUAC aerogels are synthesized from inexpensive isocyanates andhydroxyl functionalized acrylates.

In another embodiment of the invention, described herein arepolyurethane and polycarbonate aerogels, which are synthesized fromurethane-acrylate or carbonate-acrylate star monomers. In one aspect,these star monomers are stable and easy to handle, as compared tohighly-reactive isocyanates or phosgene. In another aspect, the rawmaterials used herein are inexpensive and readily available.

In another embodiment of the invention, described herein areinexpensive, multifunctional, light-weight, bendable nanoporousmaterials with high degree of flexibility. In one aspect, thesematerials may be prepared via easy, one-step synthesis methods, as willbecome apparent from the following discussion.

In another embodiment, as contemplated herein, the materials describedin this invention may be useful as multifunctional thermal and acousticinsulating materials for buildings, sub-sea oil pipes, automobiles andaircraft, and as energy absorbers for anti-ballistic applications, suchas, illustratively, armor and blast wave mitigation against improvisedexplosive devices (IEDs).

In another illustrative embodiment of the invention, the UAC Starmonomers are compounds of the formula (I):

wherein the nitrogen atoms of the urethane moieties are independentlyattached to their respective aryl rings at the 2, 3, or 4-positions ofthe aryl rings; wherein each of W, X, and Y independently represents aC₁-C₆ straight chain alkyl group or a C₁-C₆ branched alkyl group; andwherein each of R1-R9 independently represents an H, a C₁-C₆ straightchain alkyl group or a C₁-C₆ branched alkyl group. It is understood thatother related variations on the illustrative UAC Star monomers offormula (I) are contemplated herein, as will become apparent in thedetailed discussion below.

In another illustrative embodiment of the invention, the PUAC polymersare compounds of the formula (II):

wherein the nitrogen atoms of the urethane moieties are independentlyattached to their respective aryl rings at the 2, 3, or 4-positions ofthe aryl rings; wherein each of W, X, and Y independently represents aC₁-C₆ straight chain alkyl group or a C₁-C₆ branched alkyl group; andwherein each of R1-R9 independently represents an H, a C₁-C₆ straightchain alkyl group or a C₁-C₆ branched alkyl group; and wherein n is aninteger ranging upwardly from 2 upwardly to 100, 200, 500 or evenhigher. It is understood that other related variations on theillustrative PUAC polymers of formula (II) are contemplated herein, aswill become apparent in the detailed discussion below.

In another embodiment of the invention, processes are described hereinfor the conversion of the UAC Star monomers to the PUAC aerogel polymersof the invention, as will be further described in the followingdiscussion.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the ¹³C NMR spectrum of the UAC Star monomer of Example 1,in CD₃COCD₃.

FIG. 2 shows the ¹H NMR spectrum of the UAC Star monomer of Example 1,in CD₃COCD₃.

FIG. 3 shows the high resolution mass spectrum of the UAC Star monomerof Example 1.

FIG. 4 shows the solid phase ¹³C NMR spectrum of a 9-PUAC aerogel sampleprepared as described in Example 2.

FIG. 5 shows SEM images of 9-PUAC and 40-PUAC, respectively.

FIG. 6 shows a comparison of the mechanical behavior of 9-PUAC and40-PUAC aerogels. 9-PUAC: (A) Flexing, (B) after releasing the stress.40-PUAC: (C) Before compression, (D) after compression using an Instron4469 Universal Testing Machine.

FIG. 7 shows flexibility data for 9-PUAC and 40-PUAC aerogels.

FIG. 8 shows a comparative characterization by solid phase ¹³C NMR ofPUAC, PUAC-EG, and PUAC-HD.

FIG. 9 shows a comparative characterization by FTIR and TGA of PUAC,PUAC-EG, and PUAC-HD.

FIG. 10 shows a comparison of the mechanical properties of PUAC,PUAC-EG, and PUAC-HD.

FIG. 11 shows a comparison of properties of PUAC, PUAC-EG, and PUAC-HDprepared at 9% w/w concentration of Star monomer precursors.

FIG. 12 shows a comparison of particle properties of PUAC, PUAC-EG, andPUAC-HD prepared at 9% w/w concentration of Star monomer precursors.

FIG. 13 shows a comparison of properties of PUAC, PUAC-EG, and PUAC-HDprepared at 40% w/w concentration of Star monomer precursors.

FIG. 14 shows a comparison of particle properties of PUAC, PUAC-EG, andPUAC-HD prepared at 40% w/w concentration of Star monomer precursors.

FIG. 15 shows a comparison of quasi-static compression properties ofPUAC, PUAC-EG, and PUAC-HD.

FIG. 16 displays thermal conductivity properties of PUAC aerogels.

FIG. 17 describes an illustrative preparation of PUAC aerogels.

DETAILED DESCRIPTION

In one embodiment of the invention, described herein are UAC Starmonomers of the formula (I):

wherein the nitrogen atoms of the urethane moieties are independentlyattached to their respective aryl rings at the 2, 3, or 4-positions ofthe aryl rings; wherein each of W, X, and Y independently represents aC₁-C₆ straight chain alkyl group or a C₁-C₆ branched alkyl group; andwherein each of R1-R9 independently represents an H, a C₁-C₆ straightchain alkyl group or a C₁-C₆ branched alkyl group. It is understood thatother related variations on the illustrative UAC Star monomers offormula (I) are contemplated herein, as will become apparent in thedetailed discussion below. In one illustrative example, it iscontemplated herein that one or more of the urethane moieties of theforegoing UAC Star monomers of formula (I) may alternatively be replacedwith carbonate groups, urea groups, and the like. The replacement of theurethane groups of the UAC Star monomers with carbonate groups or ureagroups would provide carbonate-acrylate Star monomers or urea-acrylateStar monomers, respectively. In another illustrative example, it iscontemplated herein that one or more of the aryl rings of thetriarylmethane moiety of the UAC Star monomer of formula (I) may besubstituted with any of a variety of substituent groups known in theart, illustratively, one or more C₁-C₆ straight chain alkyl group orC₁-C₆ branched alkyl group, one or more halogen atom, one or more alkoxyor alkylthio group, one or more ether or thioether group, one or morecarboxy group, one or more ester group, one or more carboxamido group,one or more cyano group, one or more nitro group, and the like; or thatone or more of the aryl rings of the triarylmethane moiety of the UACStar monomer may be replaced with alternative aromatic or heteroaromaticrings other than benzene rings, including single-ring or fused-ringaromatics or heteroaromatics, wherein the alternative aromatic orheteroaromatic rings may be substituted with one or more of theforegoing substituents.

In another illustrative embodiment of the invention, described hereinare PUAC polymers of the formula (II):

wherein the nitrogen atoms of the urethane moieties are independentlyattached to their respective aryl rings at the 2, 3, or 4-positions ofthe aryl rings; wherein each of W, X, and Y independently represents aC₁-C₆ straight chain alkyl group or a C₁-C₆ branched alkyl group; andwherein each of R1-R9 independently represents an H, a C₁-C₆ straightchain alkyl group or a C₁-C₆ branched alkyl group; and wherein n is aninteger ranging upwardly from 2.

It is understood that other related variations on the illustrative PUACpolymers of formula (II) are contemplated herein, as will becomeapparent in the detailed discussion below. For example, one or more ofthe aryl rings of the triarylmethane moiety of the PUAC polymer offormula (II) may be substituted with any of a variety of substituentgroups known in the art, similar to the substituent groups described inthe previous paragraph in regard to the UAC Star monomers; or one ormore of the aryl rings of the triarylmethane moiety of the PUAC polymerof formula (II) may be replaced with alternative aromatic orheteroaromatic rings other than benzene rings, including single-ring orfused-ring aromatics or heteroaromatics, wherein the alternativearomatic or heteroaromatic rings may be substituted with one or more ofthe foregoing substituents.

In another embodiment of the invention, a process for the preparation ofthe UAC Star monomers of formula (I) is described herein. In oneillustrative example, the process comprises the step of reacting atris(isocyanatoaryl)methane of formula (III) with one or morehydroxyalkyl acrylate of formula (IV), in a suitable solvent or mixtureof solvents, following procedures known in the art, either with orwithout a catalyst, wherein the hydroxyl groups react with theisocyanato groups, to produce a UAC Star monomer of formula (I).Suitable solvents or mixtures of solvents for carrying out the processstep include ketone solvents such as acetone, ester solvents such asethyl acetate, and the like, or any other suitable solvents known tothose skilled in the relevant art. In the case that a catalyst is usedfor the process step, suitable catalysts include various organometallicor organic catalysts known to those skilled in the relevant art, suchas, illustratively, dibutyltin dilaurate (DBTDL). Following is anillustrative scheme of said process for preparing a UAC Star monomer offormula (I), wherein W=X=Y, R1=R4=R7, R2=R5=R8, and R3=R6=R9:

In another embodiment of the invention, a process for the preparation ofthe PUAC polymers of formula (II) is described herein. In oneillustrative example, the process comprises the step of treating asolution of a UAC Star monomer of formula (I), in a suitable solvent ormixture of solvents, with a suitable polymerization catalyst, such as,illustratively, a free radical initiator. Suitable solvents or mixturesof solvents for carrying out the process step include ketone solventssuch as acetone, ester solvents such as ethyl acetate, and the like, orany other suitable solvents known to those skilled in the relevant art.Suitable free radical initiators include any of a wide variety of agentsknown in the relevant art, such as, illustratively, the commonly usedfree radical initiator 2,2′-azobisisobutyronitrile (AIBN). In thefollowing illustrative scheme of said process for the preparation of thePUAC polymers of formula (II), wherein W=X=Y, R1=R4=R7, R2=R5=R8, andR3=R6=R9, a solution of the UAC Star monomer (I) in a suitable solventor mixture of solvents is treated with a catalytic amount of a freeradical initiator, resulting in the formation of (II):

In another embodiment of the invention, a variation on the above processfor generation of the PUAC polymers is described herein, which entailsaddition into the reaction mixture, prior to introduction of thepolymerization catalyst (e.g., the free radical initiator), of one ormore compounds termed herein as chain extenders. These chain extendersare monomeric compounds capable of copolymerizing with the UAC Starmonomers. Illustrative of these chain extenders are diacrylate compoundsof the following general formula (V):

wherein L represents a linker group selected from C₁-C₁₂ straight chainor branched chain alkyl, alkoxyalkyl, alkoxycarbonylalkyl, andalkoxycarboxyalkyl; and wherein each of R10 and R11 independentlyrepresents an H, a C₁-C₆ straight chain alkyl group or a C₁-C₆ branchedalkyl group. In one aspect of the invention, the inclusion of thesechain extenders in the polymerization step results in PUACs possessingfavorable flexibility, thermal insulation and other properties, as willbecome apparent in the discussion below. Representative of the chainextenders of the invention are compounds of the following formulae; itis to be understood that these formulae are shown only for the purposeof illustration, that they are not to be construed as limiting theinvention, and that other similar chain extenders well known to thoseskilled in the relevant art are contemplated herein:

In another embodiment of the invention, PUAC polymers are describedherein that are obtained by the above polymerization process thatincludes the addition of one or more of the chain extenders to the UACStar monomers, as described above. These PUAC polymers are similar inchemical structure to the chemical structure of the PUACs of formula(II), but include copolymerized chain extenders.

In another embodiment of the invention, a one-pot process for thepreparation of the PUAC polymers of formula (II) starting from atris(isocyanatoaryl)methane of formula (III) and one or morehydroxyalkyl acrylate of formula (IV) is described herein. In oneillustrative example, the process comprises the step of reacting atris(isocyanatoaryl)methane of formula (III) with one or morehydroxyalkyl acrylate of formula (IV), in a suitable solvent or mixtureof solvents as described above, following procedures known in the art,either with or without a catalyst, to produce a solution of thecorresponding UAC Star monomer of formula (I). This is followeddirectly, without isolation of (I), by treatment with a suitablepolymerization catalyst, such as, illustratively, a suitable freeradical initiator as described above, to produce (II). Following is anillustrative scheme of said one-pot process for the preparation of PUAC(II), wherein W=X=Y, R1=R4=R7, R2=R5=R8, and R3=R6=R9:

In another embodiment of the invention, an alternative one-pot processfor the preparation of PUAC polymers is described herein. Thisalternative one-pot process is similar in all respects to the one-potprocess described above for the preparation of the PUAC polymers offormula (II), but includes the addition into the reaction mixture, priorto introduction of the polymerization catalyst (e.g., the free radicalinitiator), of one or more of the chain extenders described above, thusresulting in PUACs that have copolymerized chain extender unitsincorporated therein.

In another embodiment of the invention, described herein are compoundsthat are derived by the electrocyclic (e.g., Diels-Alder) reaction in asuitable solvent of the alkene moiety of the hydroxyalkyl acrylate offormula (IV) with a diene, to produce the corresponding Diels-Alderadduct; wherein R1, R2, R3, and W are as defined in the foregoing.Suitable solvents for this reaction are the common solvents used in theart to carry out Diels-Alder reactions, such as toluene, the xylenes,and similar solvents. Illustrative of these compounds are thoserepresented by formula (VI), which are obtained by reaction of thehydroxyalkyl acrylate of formula (IV) with cyclopentadiene to producethe corresponding norbornene, as shown in the following scheme:

A specific example of the foregoing is the reaction of 2-hydroxyethylacrylate (i.e., compound (IV) wherein W=CH₂CH₂; R1=R2=R3=H) withcyclopentadiene to produce norbornene adduct (VI) wherein W=CH₂CH₂;R1=R2=R3=H. It is to be understood that, as contemplated herein, otherdienes may be used, including any of a plethora of non-cyclic and cyclicdienes known in the art.

In a further embodiment of the invention, Star monomers incorporatingnorbornene groups are described herein. These norbornene containing Starmonomers are obtained by the reaction of the norbornene compounds (VI)with a tris(isocyanatoaryl)methane of formula (III) under conditionsthat are similar to those described above for the reaction of (III) with(IV). Illustrative of those Star monomers that incorporate norbornenegroups are those represented by the formula (VII), which are obtained bythe reaction of the norbornene compounds (VI), wherein R1=R2=R3=H, witha tris(isocyanatoaryl)methane of formula (III), as shown in thefollowing scheme:

In another embodiment of the invention, described herein are compoundsthat are derived by the electrocyclic (e.g., Diels-Alder) reaction in asuitable solvent of the alkene moieties of hydroxyalkyl polyacrylatecompounds of formula (VIII) with a diene, to produce the correspondingDiels-Alder adduct. Suitable solvents for this reaction are the commonsolvents used in the art to carry out Diels-Alder reactions, asdescribed above. Illustrative of these compounds are those representedby formula (IX), which are obtained by reaction of the hydroxyalkylpolyacrylate compounds of formula (VIII) with cyclopentadiene to producethe corresponding adducts that contain polynorbornene moieties, as shownin the following scheme, wherein R1, R2, R3, and W are as defined in theforegoing, and m is an integer from 2 to 12:

It is to be understood that, as contemplated herein, various otherhydroxyalkyl polyacrylate compounds may be used in the Diels-Alderreaction with the various dienes (e.g., cyclopentadiene). Illustrativeof such other hydroxyalkyl polyacrylate compounds are the followingexamples represented by formulae (X) and (XI) below:

Specifically, in the case of the reaction of (X) with cyclopentadiene, aDiels-Alder adduct is obtained that contains three norbornene moieties;likewise, in the case of the reaction of (XI) with cyclopentadiene, aDiels-Alder adduct is obtained that contains five norbornene moieties.

In another embodiment of the invention, Star monomers containingmultiple norbornene groups are described herein. These Star monomers maybe obtained by the reaction of the hydroxyalkyl polynorbornene compoundsrepresented by the formula (IX) with a tris(isocyanatoaryl)methane offormula (III), under conditions similar to those described earlier.Illustratively, the polynorbornene-containing hydroxyalkyl compoundsobtained from the reactions of (X) and (XI), respectively, withcyclopentadiene are further reacted with tris(isocyanatoaryl)methane offormula (III) to produce the corresponding Star monomers.

In another embodiment of the invention, polynorbornene-polyurethane(PNUP) aerogel polymers are described herein. These PNUP aerogelpolymers are obtained via a process wherein the norbornene-containingStar monomers represented by formula (VII), or the norbornene-containingStar monomers described in the previous paragraph, are polymerized underring-opening metathesis polymerization conditions. Any of a variety ofsuitable conditions for ring-opening metathesis polymerization that arewell-known in the art may be used. Illustrative of these conditions areas follows:

First and second generation Grubbs catalysts (GC-I and GC-II) may beused,

which offer the advantages of tolerance to moisture, oxygen, proticsolvents and functional groups. GC-1 has been used in toluene, GC-II hasbeen used in toluene, acetone, tetrahydrofyran, THF and methanol.Further and alternatively, the ring-opening metathesis polymerizationprocess may be carried out in the presence of chain extenders that areknown to persons skilled in the relevant art. The followingbisnorborneneacyloxyethyl carbonate compound (XII) is illustrative ofsuch chain extenders.

In another embodiment, the aerogels of the invention herein are porous,low-density 3D assemblies of nanoparticles with large surface-to-volumeratios. In one aspect, the aerogels possess flexibility that makes themparticularly attractive materials for thermal insulation. The flexibleaerogels herein were characterized at the molecular level (solid phase¹³C NMR), nanoscopic level (SEM, SAXS), and macroscopic level(compression and 3-point bending). The lower density PUAC aerogels (0.14g cm⁻³) consist of large primary particles (88 nm in diameter) and aremacroporous and flexible. The higher density PUAC aerogels (0.66 g cm⁻³)consist of smaller particles (18 nm in diameter), and are rigid andmechanically strong.

While the novel technology herein has been illustrated and described indetail in the foregoing description, and in the following examples andfigures, the same is to be considered as illustrative and notrestrictive in character. It is understood that one of ordinary skill inthe art could readily make a nigh-infinite number of insubstantialchanges and modifications to the above-described embodiments and that itwould be impractical to attempt to describe all such embodimentvariations in the present specification. Accordingly, it is understoodthat all changes and modifications that come within the spirit of thenovel technology are desired to be protected.

Examples

The following examples further illustrate specific embodiments of theinvention. However, the following examples should not be interpreted inany way to limit the invention.

MATERIALS. All reagents and solvents were used as received unless notedotherwise. 2-Hydroxyethyl acrylate (HEA), 2,2′-azobisisobutyronitrile(AIBN) and dibutyltin dilaurate (DBTDL) were purchased fromSigma-Aldrich. Anhydrous acetone was purchased from Fisher Scientific.Siphon-grade CO₂ was purchased from Ozark Gas Co.Tris(4-isocyanatophenyl)-methane (TIPM) (27% w/w solution in ethylacetate) was obtained from Bayer Corporation USA (TIPM is referred to byBayer Corporation as Desmodur RE).

Example 1

Illustrative preparation of urethane-acrylate (UAC) Star monomers. Aurethane-acrylate Star monomer was synthesized via reaction of TIPM (1mmol) with HEA (3 mmol) using DBTDL (5 μL) as a catalyst in anhydrousacetone (see Scheme 1). The reaction mixture was stirred at roomtemperature for 30 min. The quantity of anhydrous acetone was varieddepending upon the desirable weight percent of solids in the solution.The UAC Star monomer can be isolated, recrystallized from CH₂Cl₂/hexane,and fully characterized. However, for routine preparation of aerogels,gelation was induced in one pot by adding a radical initiator, asdescribed in the following example.

The UAC Star monomer was characterized by ¹³C NMR, the spectrum of whichis shown in FIG. 1. Peak f (154 ppm) corresponds to the carbonyl groupof the urethane linkage. Peaks j and k correspond to the acrylatemoieties, which were used for free radical polymerization. The UAC Starmonomer was also characterized by ¹H NMR; the spectrum is shown in FIG.2. The UAC Star monomer was also characterized by high resolution massspectroscopy; the data is shown in FIG. 3.

Example 2

Illustrative preparation of PUAC aerogels. A UAC Star monomer wasprepared as described in the previous example. Gelation was induced inone pot by adding AIBN (0.3 mmol) into the reaction mixture containingthe UAC Star monomer, followed by transferring into molds and heating at60° C. for 2-4 h (see FIG. 17). Wet-gels were aged in their molds for 24h at 60° C., then transferred in acetone, washed 5 times, 8 h per wash,and finally were dried using SCF CO₂ to produce the PUAC aerogels.Polypropylene vials (4 mL, Wheaton polypropylene Omnivials, Part No.225402, 1 cm in diameter), or polypropylene centrifuge tubes (50 mL,Fisher Scientific, Cat. No. 06-443-18, 2.8 cm in diameter) were used asmolds. The PUAC aerogels are referred to herein as ‘xx-PUAC’, where ‘xx’denotes percent weight of monomers in the solution.

Solid phase ¹³C NMR was used to confirm formation of the PUAC polymerand to determine whether all the double bonds of the Star monomer hadreacted by free radical polymerization. FIG. 4 shows the solid phase ¹³CNMR of a 9-PUAC prepared as described above. The relative ratio ofaromatic carbons (110-145 ppm) to aliphatic carbons (20-75 ppm) wasfound to be close to the theoretical value (1.31:1.00 vs 1.38:1.00,respectively), thus confirming complete reaction.

Example 3

Comparison of PUAC aerogels from the lowest Star monomer concentration(9-PUAC) with PUAC aerogels from the highest Star monomer concentration(40-PUAC). The PUACs were prepared as described in the previous example.It was found that 9-PUACs were flexible, while 40-PUACs were rigid. TheSEM images of 9-PUAC and 40-PUAC are displayed in FIG. 5, which show thefollowing data: SEM of 9-PUAC: ρ_(b)=0.135±0.004 g cm⁻³, porosity=90%v/v; SEM of 40-PUAC: ρ_(b)=0.662±0.004 g cm⁻³, porosity=50% v/v. Atlower monomer concentrations, the polymer chains are expected to growlonger resulting late phase separation and formation of larger primaryparticles (88 nm in diameter by SAXS for 9-PUAC). At higher monomerconcentrations, early phase separation leads to formation of smallerprimary particles (18 nm in diameter by SAXS for 40-PUAC). Aggregationof primary particles in case of 40-PUAC yields clusters of secondary andtertiary particles (by SAXS). Therefore, 9-PUAC aerogels have lowerinter-particle connectivity than 40-PUAC.

Example 4

Comparison of the Mechanical Behavior of 9-PUAC and 40-PUAC aerogels. Acomparison of the mechanical behavior of 9-PUAC and 40-PUAC aerogels isshown in FIG. 6: 9-PUAC: (A) Flexing, (B) after releasing the stress.40-PUAC: (C) Before compression, (D) after compression using an Instron4469 Universal Testing Machine. It was found that 9-PUAC is flexible andwhen stress is released, it practically recovers its original shape.

Example 5

Flexibility of PUAC Aerogels. The flexibility of 9-PUAC was formallycharacterized with 3-point bending using a Dynamic Mechanical Analyzer(FIG. 7). (A) Stress-strain curves of 9-PUAC aerogels via a 3-pointbending test (3 samples—only the early part of the curve is shown). (B)Stress-strain curves of 40-PUAC aerogels via compression testing (3samples—only the early part of the curve is shown). With a higherinter-particle connectivity, 40-PUAC aerogels are rigid and mechanicallystrong (see FIG. 6D). The ultimate compressive strength, the compressiveYoung's modulus and the specific energy absorption were found to beequal to 175 MPa, 370 MPa and 45 J g⁻¹, respectively (see FIG. 7B).

Example 6

Illustrative preparation of PUAC aerogels with inclusion ofethyleneglycol dimethacrylate (EGDMA) or hexamethylene diacrylate (HMDA)as chain extenders. A UAC Star monomer was prepared exactly as describedin Example 1 above. EGDMA or HMDA (0.75 mmol) was added to the UAC Starmonomer solution. Gelation with AIBN, and subsequent aging of thewet-gels in molds, and drying using SCF CO₂ were done exactly asdescribed in the procedure of Example 2 above. This provided the desiredethyleneglycol diacrylate extended PUAC (PUAC-EG) or the hexamethylenediacrylate extended PUAC (PUAC-HD).

Example 7

Comparative characterization by solid phase ¹³C NMR of PUAC, PUAC-EG,and PUAC-HD. FIG. 8 shows the comparative ¹³C NMR spectra of PUAC,PUAC-EG, and PUAC-HD, showing that the chain extenders have beenincorporated in the material in the prescribed molar ratio.

Example 8

Comparative characterization by FTIR and thermogravimetric analysis(TGA) of PUAC, PUAC-EG, and PUAC-HD. FIG. 9 shows a comparison of theFTIR spectra and TGA traces of PUAC, PUAC-EG, and PUAC-HD, showing thechain extenders do not alter substantially the functional groupfootprint or the thermal behavior of the basic PUAC materials.

Example 9

Comparative mechanical characterization of PUAC, PUAC-EG, and PUAC-HD.FIG. 10 shows a comparison of the mechanical properties of PUAC,PUAC-EG, and PUAC-HD, showing that chain extenders change substantiallythe flexural moduli of the maerial, but not its compressive behavior.

Example 10

Comparison of properties of PUAC, PUAC-EG, and PUAC-HD prepared at 9%w/w concentration of Star monomer precursors. FIG. 11 displays variouscomparative properties related to the porous structure of the PUAC,PUAC-EG, and PUAC-HD prepared at 9% w/w concentration of Star monomerprecursors. For comparative bulk densities, progressively longer chainextenders give larger particles and significantly reduced surface areas.

Example 11

Comparison of particle properties of PUAC, PUAC-EG, and PUAC-HD preparedat 9% w/w concentration of Star monomer precursors. FIG. 12 displayscomparative particle sizes determined with small angle x-ray scatteringand SEM of the PUAC, PUAC-EG, and PUAC-HD prepared at 9% w/wconcentration of Star monomer precursors, showing a generally goodagreement between primary particle sizes with those calculated from gassorption data (refer to FIG. 11), indicating absence of closed porosity.

Example 12

Comparison of properties of PUAC, PUAC-EG, and PUAC-HD prepared at 40%w/w concentration of Star monomer precursors. FIG. 13 displays variouscomparative properties related to the porous structure of the PUAC,PUAC-EG, and PUAC-HD prepared at 40% w/w concentration of Star monomerprecursors. For comparative bulk densities, particle sizes are notaffected by the presence of chain extenders.

Example 13

Comparison of particle properties of PUAC, PUAC-EG, and PUAC-HD preparedat 40% w/w concentration of Star monomer precursors. FIG. 14 displayscomparative particle sizes determined with small angle x-ray scatteringand SEM of the PUAC, PUAC-EG, and PUAC-HD prepared at 40% w/wconcentration of Star monomer precursors, showing a generally goodagreement between primary particle sizes with those calculated from gassorption data (refer to FIG. 13), indicating absence of closed porosity

Example 14

Comparison of quasi-static compression properties of PUAC, PUAC-EG, andPUAC-HD. FIG. 15 displays comparative quasi-static compression data ofPUAC, PUAC-EG, and PUAC-HD. For comparative densities, the Young'smodulus decreases and flexibility increases for longer chain extenders,but the overall energy absorption capability remains about the same.

Example 15

Thermal conductivity properties of PUAC aerogels. FIG. 16 displaysthermal conductivity data of PUAC aerogels. On the left, it shows rawdata of heat transfer across an aerogel disk using a laser flash method.On the right, it shows the variation of thermal conductivity, X, withbulk density. 20-PUAC samples are about as good thermal insulators asglass wool (0.047 versus 0.040 W m⁻¹ K⁻¹).

Example 16

Illustrative preparation of Star monomers containing norbornene groups.To a solution of 2-hydroxyethyl acrylate in toluene is added a solutionof cyclopentadiene in toluene, the mixture is stirred under conditionsknown in the art to be suitable for Diels-Alder reaction, and thereaction between the alkene and diene is monitored until formation ofthe Diels-Alder adduct is complete. The resultant norbornene-containinghydroxyl compound is isolated using standard organic chemistryprocedures. Subsequently, this norbornene-containing hydroxyl compoundis subjected to reaction with TIPM in the presence of DBTDL as acatalyst in anhydrous acetone, following the procedure described inExample 1 above, thus producing the correspondingtris(norbornene)-containing Star monomer.

Additional examples of the preparation of norbornene-containing Starmonomers following the procedure described herein are displayed in thefollowing scheme, wherein n is an integer that is equal to 3, 9, or 15.The polynorbornene-containing Star monomer 15-NB shown below is obtainedin the case where n=15:

What is claimed is:
 1. A norbornene-containing star monomer formed bythe reaction of a norbornene-containing hydroxyl compound of the formula(IX)

with a tris(isocyanatophenyl)methane of formula (III)

wherein W is a C₁-C₆ straight chain or branched alkyl or alkoxyalkylgroup; wherein R1, R2, and R3 are each independently hydrogen or C₁-C₆straight chain or branched alkyl group; and, wherein m is an integerfrom 1 to
 5. 2. A process for preparing the norbornene-containing starmonomer of claim 1, the process comprising the step of mixing atris(isocyanatophenyl)methane of formula (III) with three molarequivalents of the norbornene-containing hydroxyl compound of formula(IX) in an organic solvent.
 3. The process of claim 2, furthercomprising the addition of a catalyst.
 4. The process of claim 3,wherein the catalyst is an organotin compound.
 5. The process of claim4, wherein the organotin compound is dibutyltin dilaurate.
 6. Theprocess of claim 2 wherein the organic solvent is selected from thegroup consisting of a ketone solvent, an ester solvent, and acombination thereof.
 7. The process of claim 6, wherein the organicsolvent is acetone, ethyl acetate, or a combination thereof.
 8. Thenorbornene-containing star monomer of claim 1, wherein, in thenorbornene-containing hydroxyl compound of formula (IX), R1=R2=R3=H,W=CH₂CH₂, and m=1; and, wherein, in the tris(isocyanatophenyl)methane offormula (III), the nitrogen atoms of the isocyanate groups are attachedto their respective aryl rings at the 4-positions of the aryl rings. 9.A polynorbornene-polyurethane polymer formed by polymerization of anorbornene-containing star monomer obtained by the reaction of anorbornene-containing hydroxyl compound of the formula (IX)

with a tris(isocyanatophenyl)methane of formula (III)

wherein W is a C₁-C₆ straight chain or branched alkyl or alkoxyalkylgroup; wherein R1, R2, and R3 are each independently hydrogen or C₁-C₆straight chain or branched alkyl group; and, wherein m is an integerfrom 1 to
 5. 10. The polynorbornene-polyurethane polymer of claim 9,wherein, in the compound of formula (IX), R1=R2=R3=H, W=CH₂CH₂, and m=1;and, wherein, in the tris(isocyanatophenyl)methane of formula (III), thenitrogen atoms of the isocyanate groups are attached to their respectivearyl rings at the 4-positions of the aryl rings.
 11. Apolynorbornene-polyurethane polymer formed by copolymerization of anorbornene-containing star monomer with a dinorbornene-containing chainextender, wherein the norbornene-containing star monomer is obtained bythe reaction of a norbornene-containing hydroxyl compound of the formula(IX)

with a tris(isocyanatophenyl)methane of formula (III)

wherein W is a C₁-C₆ straight chain or branched alkyl or alkoxyalkylgroup; wherein R1, R2, and R3 are each independently hydrogen or C₁-C₆straight chain or branched alkyl group; and, wherein m is an integerfrom 1 to
 5. 12. The polynorbornene-polyurethane polymer of claim 11,wherein the dinorbornene-containing chain extender is a compound of theformula (XII):


13. The polynorbornene-polyurethane polymer of claim 9 or claim 11,wherein the polymerization is ring-opening metathesis polymerization.14. The polynorbornene-polyurethane polymer of claim 11, wherein, in thecompound of formula (IX), R1=R2=R3=H, W=CH₂CH₂, and m=1; and, wherein,in the tris(isocyanatophenyl)methane of formula (III), the nitrogenatoms of the isocyanate groups are attached to their respective arylrings at the 4-positions of the aryl rings.
 15. Thepolynorbornene-polyurethane polymer of claim 9 or claim 11, wherein saidpolymerization is carried out under ring-opening metathesispolymerization conditions.
 16. The polynorbornene-polyurethane polymerof claim 9 or claim 11, wherein the polymer is an aerogel.